Literature DB >> 15608506

Pheochromocytoma and functional paraganglioma.

Heather Yeo1, Sanziana Roman.   

Abstract

PURPOSE OF REVIEW: Pheochromocytoma is a rare, but clinically important tumor of chromaffin cells. Advances in our understanding of the genetic alterations causing hereditary forms and the increasing sensitivity of biochemical assays allow for early identification of high risk individuals and families. Surgical intervention remains the treatment of choice for patients with pheochromocytoma. This article reviews recent developments in the diagnosis, treatment, and pathophysiology of pheochromocytoma, with the objective of developing new guidelines in the identification and management of the disease. It emphasizes current diagnostic and surgical approaches and discusses the potential for future developments in the field.
SUMMARY: Advances in the molecular basis of pheochromocytoma have introduced new diagnostic modalities. Refinements in imaging techniques have improved the rate of detection of metastatic disease. Innovations in surgical techniques and trials of adrenal sparing surgery may find a niche in the surgical armamentarium.

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Year:  2005        PMID: 15608506     DOI: 10.1097/01.cco.0000147900.12325.d9

Source DB:  PubMed          Journal:  Curr Opin Oncol        ISSN: 1040-8746            Impact factor:   3.645


  19 in total

1.  [An incidental finding of retrocaval extraadrenal pheochromocytoma].

Authors:  Katharina Maria Bretterbauer; Daniela Colleselli; Ahmed Magdy; Günter Janetschek; Michael Mitterberger
Journal:  Wien Med Wochenschr       Date:  2015-07-14

2.  Simultaneous adrenal pheochromocytoma and carotid body paraganglioma in a woman.

Authors:  Eun Ji Han; Sang-Hoon Lee; In Uk Song; Yong-An Chung; Lee-So Maeng
Journal:  Nucl Med Mol Imaging       Date:  2012-10-16

3.  Heart combined with adrenal multiple pheochromocytomas.

Authors:  Su-Hong Zhao; Shuang Liang; Jing Luo; Hong-Dan Mo; Yu Jiang; Mao-Mao Zhang; Jie Yuan
Journal:  J Nucl Cardiol       Date:  2017-06-07       Impact factor: 5.952

4.  Clinical experience with pheochromocytoma in a single centre over 16 years.

Authors:  Dario Cotesta; Luigi Petramala; Valentina Serra; Mario Pergolini; Eleonora Crescenzi; Laura Zinnamosca; Giorgio De Toma; Antonio Ciardi; Iacopo Carbone; Rita Massa; Sebastiano Filetti; Claudio Letizia
Journal:  High Blood Press Cardiovasc Prev       Date:  2013-01-03

Review 5.  [Pheochromocytoma - still a challenge].

Authors:  N Reisch; M K Walz; Z Erlic; H P H Neumann
Journal:  Internist (Berl)       Date:  2009-01       Impact factor: 0.743

6.  Hypertension in a teenager: a family affair.

Authors:  Sukhpreet Singh Dubb; Asiya Tafader; Karim Meeran; Jeremy Fletcher
Journal:  BMJ Case Rep       Date:  2014-01-15

7.  131I-MIBG therapy in metastatic phaeochromocytoma and paraganglioma.

Authors:  Gonca Kara Gedik; Cornelis A Hoefnagel; Evert Bais; Renato A Valdés Olmos
Journal:  Eur J Nucl Med Mol Imaging       Date:  2007-12-11       Impact factor: 9.236

8.  Comparison of free plasma metanephrines enzyme immunoassay with (131)I-MIBG scan in diagnosis of pheochromocytoma.

Authors:  Yun-Chao Gao; Han-Kui Lu; Quan-Yong Luo; Li-Bo Chen; Ying Ding; Rui-Sen Zhu
Journal:  Clin Exp Med       Date:  2008-07-11       Impact factor: 3.984

9.  Acrocyanosis in a young adult: a rare presentation of extra-adrenal pheochromocytoma.

Authors:  Prabhat Kumar; Soumik Ghosh; Hitendra Singh Tanwar; Ashish Kumar Gupta
Journal:  BMJ Case Rep       Date:  2014-05-28

10.  Clinicopathological analysis of paraganglioma with literature review.

Authors:  Ning Feng; Wen-Yan Zhang; Xiao-Ting Wu
Journal:  World J Gastroenterol       Date:  2009-06-28       Impact factor: 5.742

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